Determination of remifentanil in neonatal dried blood spots by liquid chromatography-tandem mass spectrometry.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Acta Pharmaceutica Pub Date : 2024-05-30 Print Date: 2024-06-01 DOI:10.2478/acph-2024-0010
Jurij Trontelj, Aleš Rozman, Aleš Mrhar
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引用次数: 0

Abstract

Remifentanil is an ultra-short-acting synthetic opioid-class analgesic which might be increasingly used "off-label" as pain management during labour. Side effects in parturients during labour, and in the infant at birth are of particular concern, especially respiratory depression which is concentration-dependent, and can occur at levels as low as 3-5 ng mL-1. The safety of such use, particularly in newborns due to remifentanil placental transfer, has not been fully demonstrated yet, partly due to the lack of a suitable non-invasive analytical method. The aim of our work was to develop a sensitive method to monitor the levels of remifentanil in neonates by a non-invasive sampling of umbi lical cord blood to support efficacy and safety trials. The presented LC-MS method is sensitive enough to reliably quantify remifentanil in just 20 µL of blood at only 0.3 ng mL-1. The dried blood spot sample preparation included solvent extraction with subsequent solid-phase extraction. The method was validated in terms of accuracy, precision, recovery, matrix effect, and stability, and was successfully applied to a small pilot study. The estimated arterial blood concentrations at the time of delivery ranged from 0.2 to 0.3, and up to 0.9 ng mL-1 in neonatal, and maternal samples, respectively.

利用液相色谱-串联质谱法测定新生儿干血点中的瑞芬太尼。
雷米芬太尼是一种超短效合成阿片类镇痛药,可能越来越多地被 "标签外 "用于分娩镇痛。这种药物在分娩过程中对产妇和婴儿产生的副作用尤其令人担忧,尤其是呼吸抑制,这种副作用与浓度有关,在低至 3-5 纳克毫升/升时就会出现。使用这种药物的安全性,尤其是瑞芬太尼胎盘转移对新生儿的影响,尚未得到充分证实,部分原因是缺乏合适的无创分析方法。我们的工作旨在开发一种灵敏的方法,通过对脐带血进行无创采样来监测新生儿体内的瑞芬太尼水平,以支持疗效和安全性试验。所介绍的 LC-MS 方法灵敏度高,能可靠地定量检测 20 µL 血液中瑞芬太尼的含量,仅为 0.3 纳克 mL-1。干血斑样品的制备包括溶剂萃取和固相萃取。该方法在准确度、精密度、回收率、基质效应和稳定性等方面都得到了验证,并成功应用于一项小型试验研究。在新生儿和产妇样本中,分娩时动脉血中的估计浓度分别为 0.2 至 0.3 纳克毫升-1 和高达 0.9 纳克毫升-1。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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